Abstract
The exocyst is a multiprotein complex essential for tethering secretory vesicles to specific domains of the plasma membrane for exocytosis1,2,3. Here, we report that the exocyst component Exo70 interacts with the Arp2/3 complex, a key regulator of actin polymerization4,5. We further show that the exocyst–Arp2/3 interaction is regulated by epidermal growth factor (EGF) signalling. Inhibition of Exo70 by RNA interference (RNAi) or antibody microinjection blocks the formation of actin-based membrane protrusions and affects various aspects of cell motility. We propose that Exo70, in addition to functioning in exocytosis, also regulates actin at the leading edges of migrating cells, therefore coordinating cytoskeleton and membrane traffic during cell migration.
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Acknowledgements
We thank T. Svitkina, M. Welch, B. Goode, S. Zigmond, M. Chou, J. Peterson and C. Yang for reagents and numerous constructive discussions during the research. This work is supported by the National Institutes of Health (NIH), the American Cancer Society (ACS), the American Heart Association (AHA) and the Pew Scholars Program for Biomedical Sciences to W.G.
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Zuo, X., Zhang, J., Zhang, Y. et al. Exo70 interacts with the Arp2/3 complex and regulates cell migration. Nat Cell Biol 8, 1383–1388 (2006). https://doi.org/10.1038/ncb1505
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DOI: https://doi.org/10.1038/ncb1505